石墨烯
材料科学
氧化物
塔菲尔方程
化学工程
碳纳米管
硫黄
多硫化物
纳米颗粒
成核
热解
碳纤维
钴
锂(药物)
纳米技术
电化学
电极
复合数
化学
复合材料
有机化学
冶金
物理化学
内分泌学
工程类
医学
电解质
作者
Jeong Yeon,Young Hun Ko,Tae Ho Park,Hyunyoung Park,Jongsoon Kim,Ho Seok Park
出处
期刊:Energy & environmental materials
日期:2021-03-15
卷期号:5 (2): 555-564
被引量:53
摘要
Lithium–sulfur batteries (LSBs) are regarded as promising candidates for the next‐generation energy storage devices owing to their high‐theoretical capacity (1675 mAh g −1 ) and affordable cost. However, several limitations of LSBs such as the lithium polysulfide shuttle, large volume expansion, and low electrical conductivity of sulfur need to be resolved for practical applications. To address these limitations, herein, a multidimensional architectured hybrid (Co@CNT/nG), where Co 3 O 4 nanoparticles are encapsulated into three‐dimensional (3D) porous N‐doped reduced graphene oxide interconnected with carbon nanotube (CNT) branches, is synthesized through a simple pyrolysis method. The synergistic effect achieved through the homogeneously distributed and encapsulated Co 3 O 4 nanoparticles, the interconnected CNT branches, and the 3D hierarchical porous structure and N‐doping of Co@CNT/nG significantly suppresses the shuttle effect of lithium polysulfides and enhances the conversion redox kinetics for the improved sulfur utilization. We validate this effect through various measurements including symmetric cells, Li 2 S nucleation, shuttle currents, Tafel slopes, diffusion coefficients, and post‐mortem analyses. Importantly, Co@CNT/nG‐70S‐based LSB cells achieve a high‐specific capacity of 1193.1 mAh g −1 at 0.1 C and a low capacity decay rate of 0.030% per cycle for 700 cycles at 5 C, delivering a high areal capacity of 5.62 mAh cm −2 even with a loading of 6.5 mg cm −2 .
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